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FULL-MDS: Fluorescent Universal Lipid Labeling for Microfluidic Diffusional Sizing
[Image: see text] Microfluidic diffusional sizing (MDS) is a recent and powerful method for determining the hydrodynamic sizes and interactions of biomolecules and nanoparticles. A major benefit of MDS is that it can report the size of a fluorescently labeled target even in mixtures with complex, un...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850350/ https://www.ncbi.nlm.nih.gov/pubmed/36574263 http://dx.doi.org/10.1021/acs.analchem.2c03168 |
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author | Baron, Jasmin Bauernhofer, Lena Devenish, Sean R. A. Fiedler, Sebastian Ilsley, Alison Riedl, Sabrina Zweytick, Dagmar Glueck, David Pessentheiner, Ariane Durand, Grégory Keller, Sandro |
author_facet | Baron, Jasmin Bauernhofer, Lena Devenish, Sean R. A. Fiedler, Sebastian Ilsley, Alison Riedl, Sabrina Zweytick, Dagmar Glueck, David Pessentheiner, Ariane Durand, Grégory Keller, Sandro |
author_sort | Baron, Jasmin |
collection | PubMed |
description | [Image: see text] Microfluidic diffusional sizing (MDS) is a recent and powerful method for determining the hydrodynamic sizes and interactions of biomolecules and nanoparticles. A major benefit of MDS is that it can report the size of a fluorescently labeled target even in mixtures with complex, unpurified samples. However, a limitation of MDS is that the target itself has to be purified and covalently labeled with a fluorescent dye. Such covalent labeling is not suitable for crude extracts such as native nanodiscs directly obtained from cellular membranes. In this study, we introduce fluorescent universal lipid labeling for MDS (FULL-MDS) as a sparse, noncovalent labeling method for determining particle size. We first demonstrate that the inexpensive and well-characterized fluorophore, Nile blue, spontaneously partitions into lipid nanoparticles without disrupting their structure. We then highlight the key advantage of FULL-MDS by showing that it yields robust size information on lipid nanoparticles in crude cell extracts that are not amenable to other sizing methods. Furthermore, even for synthetic nanodiscs, FULL-MDS is faster, cheaper, and simpler than existing labeling schemes. |
format | Online Article Text |
id | pubmed-9850350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98503502023-01-20 FULL-MDS: Fluorescent Universal Lipid Labeling for Microfluidic Diffusional Sizing Baron, Jasmin Bauernhofer, Lena Devenish, Sean R. A. Fiedler, Sebastian Ilsley, Alison Riedl, Sabrina Zweytick, Dagmar Glueck, David Pessentheiner, Ariane Durand, Grégory Keller, Sandro Anal Chem [Image: see text] Microfluidic diffusional sizing (MDS) is a recent and powerful method for determining the hydrodynamic sizes and interactions of biomolecules and nanoparticles. A major benefit of MDS is that it can report the size of a fluorescently labeled target even in mixtures with complex, unpurified samples. However, a limitation of MDS is that the target itself has to be purified and covalently labeled with a fluorescent dye. Such covalent labeling is not suitable for crude extracts such as native nanodiscs directly obtained from cellular membranes. In this study, we introduce fluorescent universal lipid labeling for MDS (FULL-MDS) as a sparse, noncovalent labeling method for determining particle size. We first demonstrate that the inexpensive and well-characterized fluorophore, Nile blue, spontaneously partitions into lipid nanoparticles without disrupting their structure. We then highlight the key advantage of FULL-MDS by showing that it yields robust size information on lipid nanoparticles in crude cell extracts that are not amenable to other sizing methods. Furthermore, even for synthetic nanodiscs, FULL-MDS is faster, cheaper, and simpler than existing labeling schemes. American Chemical Society 2022-12-27 /pmc/articles/PMC9850350/ /pubmed/36574263 http://dx.doi.org/10.1021/acs.analchem.2c03168 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Baron, Jasmin Bauernhofer, Lena Devenish, Sean R. A. Fiedler, Sebastian Ilsley, Alison Riedl, Sabrina Zweytick, Dagmar Glueck, David Pessentheiner, Ariane Durand, Grégory Keller, Sandro FULL-MDS: Fluorescent Universal Lipid Labeling for Microfluidic Diffusional Sizing |
title | FULL-MDS: Fluorescent
Universal Lipid Labeling for
Microfluidic Diffusional Sizing |
title_full | FULL-MDS: Fluorescent
Universal Lipid Labeling for
Microfluidic Diffusional Sizing |
title_fullStr | FULL-MDS: Fluorescent
Universal Lipid Labeling for
Microfluidic Diffusional Sizing |
title_full_unstemmed | FULL-MDS: Fluorescent
Universal Lipid Labeling for
Microfluidic Diffusional Sizing |
title_short | FULL-MDS: Fluorescent
Universal Lipid Labeling for
Microfluidic Diffusional Sizing |
title_sort | full-mds: fluorescent
universal lipid labeling for
microfluidic diffusional sizing |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850350/ https://www.ncbi.nlm.nih.gov/pubmed/36574263 http://dx.doi.org/10.1021/acs.analchem.2c03168 |
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